Canonical Allele Identifier: CA10573064

Gene: USP9Y

Linked Data

• dbSNP Id: rs772156837
• ExAC: Y:14847654 CTTA / C
• gnomAD v2: Y-14847654-CTTA-C
• MyVariant Identifiers: chrY:g.14847655_14847657del (hg19) ; chrY:g.12735721_12735723del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12735724_12735726del , CM000686.2:g.12735724_12735726del	GRCh38
NC_000024.9:g.14847658_14847660del , CM000686.1:g.14847658_14847660del	GRCh37
NC_000024.8:g.13357052_13357054del	NCBI36
NG_008311.1:g.39499_39501del

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.770_772del	ENSP00000498372.1:p.Ile257del
ENST00000338981.7:c.770_772del MANE Select	ENSP00000342812.3:p.Ile257del
ENST00000426564.6:n.782_784del
NM_004654.3:c.770_772del	NP_004645.2:p.Ile257del
XM_011531469.1:c.770_772del	XP_011529771.1:p.Ile257del
XM_011531470.1:c.519+17_519+19del	XP_011529772.1:n.519+17_519+19del
XM_017030078.2:c.770_772del	XP_016885567.1:p.Ile257del
NM_004654.4:c.770_772del MANE Select	NP_004645.2:p.Ile257del